Rechercher

CISPR 35:2016 applies to multimedia equipment (MME) having a rated AC or DC supply voltage not exceeding 600 V. The objectives of this document are: - to establish requirements which provide an adequate level of intrinsic immunity so that the MME will operate as intended in its environment in the frequency range 0 kHz to 400 GHz; and - to specify procedures to ensure the reproducibility of…

La CISPR 35:2016 s'applique aux équipements multimédia (MME) dont la tension d'alimentation assignée en courant alternatif ou en courant continu ne dépasse pas 600 V. Les objectifs du présent document sont: - d'établir des exigences qui fournissent un niveau suffisant d'immunité intrinsèque, permettant aux MME de fonctionner comme prévu dans leur environnement dans la plage…

IEC 61169-58:2016, which is a sectional specification (SS), provides information and rules for the preparation of detail specifications (DS) for SBMA series coaxial connectors with blind-mate coupling. The connectors are used with cables with characteristic impedance 50 Ω in an operating frequency range up to 28 GHz. The connectors are widely used in communications, antennas, radars and other…

L'IEC 61169-58:2016, qui est une spécification intermédiaire (SI), fournit des informations et des règles en vue de l'établissement de spécifications particulières (SP) relatives aux connecteurs coaxiaux de série SBMA à accouplement en aveugle. Les connecteurs sont utilisés avec des câbles d'une impédance caractéristique de 50 Ω dans une plage de fréquences de fonctionnement allant…

IEC TR 63036:2016(E) specifies the electrical interface and test procedures for the control by mains voltage phase-cut dimming of the brightness of mains operated electronic lighting equipment intended to be controlled by mains voltage phase-cut dimmers, such as LED integrated lamps, and light sources with external control gear. Electronic switches that use a comparable circuitry to a phase-cut…

ISO 15674:2016 specifies requirements for sterile, single-use, extracorporeal hard-shell cardiotomy/venous reservoir systems and soft venous reservoir bags intended for use as a blood reservoir during cardiopulmonary bypass (CPB) surgery. It applies only to the blood reservoir aspects for multifunctional systems which can have integral parts such as blood-gas exchangers (oxygenators), blood…

ISO 15675:2016 specifies requirements for sterile, single-use, arterial blood line filters intended to filter and remove emboli, debris, blood clots and other potentially hazardous solid and gaseous material from the blood of humans during cardiopulmonary bypass surgery.

ISO 15676:2016 specifies requirements for single-use tubing packs for cardiopulmonary bypass and extracorporeal membrane oxygenation (ECMO). This document is applicable to all medical tubing intended for cardiopulmonary bypass (CPB) and/or extracorporeal membrane oxygenation (ECMO), but specific requirements and tests are included for tubing intended for use with peristaltic pumps during (short-…

ISO 18241:2016 specifies requirements for sterile, single-use, venous bubble traps intended to remove air entering the venous line during surgical procedures requiring extracorporeal circulatory support, which may include cardiopulmonary bypass (CPB), extracorporeal membrane oxygenation (ECMO), or venovenous bypass for liver transplantation.

ISO 18746:2016 specifies the requirements of sterile intradermal acupuncture needle for single use as a medical device, including the following factors: a) size; b) material; c) quality; d) testing methods; e) packing; f) identification.